Ziprasidone hydrochloride monohydrate
A full antagonist of D2 and 5-HT2A receptors with Ki of 6.8 and 0.6 nM, respectively; also is a partial agonist of 5-HT1A, and a partial antagonist of 5-HT2C and 5-HT1D receptors; exhibits potent antipsychotic activity in vivo.Schizophrenia Approved (In Vitro) :Ziprasidone hydrochloride monohydrate (0-500 nM, 150 seconds) blocks wild-type hERG current. (In Vivo) :Ziprasidone hydrochloride monohydrate (oral gavage; 20 mg/kg; once daily; 7 weeks) results in weight loss, low level physical activity, high resting energy expenditure and greater capacity for thermogenesis when subjected to cold.
Product Specifications
CAS Number
138982-67-9
Product Name Alternative
CP-88059
Field of Research
Pharmacology & Drug Discovery
Purity
>98% (HPLC)
Solubility
10 mM in DMSO
Smiles
O=C1CC2=CC (CCN3CCN (C4=NSC5=C4C=CC=C5) CC3) =C (Cl) C=C2N1.Cl.O
Molecular Formula
C21H24Cl2N4O2S
Molecular Weight
467.4119
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
2H-Indol-2-one, 5-[2-[4- (1,2-benzisothiazol-3-yl) -1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
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